US2006166241A1PendingUtilityA1
Nucleic acid isolation unit and method using intercalator
Est. expiryJan 25, 2025(expired)· nominal 20-yr term from priority
Inventors:Jeo-Young ShimKyu-Youn HwangJoon-Ho KimSung-Ouk JungKyu-Tae YooJoon Shik ParkJi-Na Namgoong
C12Q 1/6844C12Q 2523/308C12N 15/1006C12Q 2563/173C12Q 1/6806
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Abstract
Provided are nucleic acid isolation unit and method. The method includes immobilizing an aromatic compound-containing nucleic acid intercalator on a solid support; contacting a first buffer solution containing a nucleic acid sample to be purified to the intercalator immobilized on the solid support to bind the intercalator with nucleic acids contained in the nucleic acid sample; cleaning the resultant structure where the nucleic acids are bound to the intercalator immobilized on the solid support; and eluting the nucleic acids with a second buffer solution.
Claims
exact text as granted — not AI-modified1 . A nucleic acid isolation unit comprising:
a solid support; a polymer layer coated on the solid support; and a nucleic acid intercalator comprising an aromatic compound immobilized on the polymer layer.
2 . The nucleic acid isolation unit of claim 1 , wherein the solid support is in the form of a plate or a bead.
3 . The nucleic acid isolation unit of claim 1 , wherein the polymer layer comprises at least one functional group selected from the group consisting of a hydroxy group, an amino group, a thiol group, a carboxy group, an alkoxy group, and a formyl group.
4 . The nucleic acid isolation unit of claim 1 , wherein the polymer layer comprises at least one polymer selected from the group consisting of polysilane, polyalcohol, polyvinyl, and polystyrene.
5 . The nucleic acid isolation unit of claim 1 , wherein the nucleic acid intercalator is covalently bound to the polymer layer.
6 . The nucleic acid isolation unit of claim 1 , wherein the nucleic acid intercalator is a substituted or unsubstituted aromatic compound of 10 to 100 carbon atoms.
7 . The nucleic acid isolation unit of claim 6 , wherein the aromatic compound has 2 to 6 benzene rings and the benzene rings are attached to each other as a pendant group or are partially or wholly fused.
8 . The nucleic acid isolation unit of claim 6 , wherein the aromatic compound is at least one selected from the group consisting of naphthalene, anthracene, phenanthrene, pyrene, chrysene, and tetracene.
9 . A nucleic acid isolation method using an intercalator comprising:
immobilizing an aromatic compound-containing nucleic acid intercalator on a solid support; contacting a first buffer solution containing a nucleic acid sample to be purified to the intercalator immobilized on the solid support to bind the intercalator with nucleic acids contained in the nucleic acid sample; cleaning the resultant structure where the nucleic acids are bound to the intercalator immobilized on the solid support; and eluting the nucleic acids with a second buffer solution.
10 . The nucleic acid isolation method of claim 9 , wherein the nucleic acid intercalator is a substituted or unsubstituted aromatic compound of 10 to 100 carbon atoms.
11 . The nucleic acid isolation method of claim 10 , wherein the aromatic compound has 2 to 6 benzene rings and the benzene rings are attached to each other as a pendant group or are partially or wholly fused.
12 . The nucleic acid isolation method of claim 10 , wherein the aromatic compound is at least one selected from the group consisting of naphthalene, anthracene, phenanthrene, pyrene, chrysene, and tetracene.
13 . The nucleic acid isolation method of claim 9 , wherein the nucleic acids are double-stranded DNAs or single-stranded DNAs.
14 . The nucleic acid isolation method of claim 9 , wherein the first buffer solution has a salt concentration of 0.1 to 0.3M.
15 . The nucleic acid isolation method of claim 9 , wherein the second buffer solution has a salt concentration of 0.5 to 2M.
16 . The nucleic acid isolation method of claim 9 , wherein the second buffer solution is a nucleic acid amplification buffer.
17 . The nucleic acid isolation method of claim 16 , wherein the nucleic acid amplification buffer is a PCR (Polymerase Chain Reaction) buffer.
18 . The nucleic acid isolation method of claim 9 , wherein the second buffer solution has a temperature of 70 to 100° C.Cited by (0)
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